2nd Shift - Process Engineer III

Johnson & Johnson Innovative Medicine•Memphis, TN

About The Position

The Process Engineer III provides technical leadership for process improvement, equipment reliability, validation, and compliance within a regulated medical supply chain facility. The role uses engineering expertise, data-driven problem-solving, and cross-functional collaboration to improve safety, quality, capacity, uptime, and product flow while reducing operational risk and ensuring reliable service to customers and patients. The position serves as the process engineering technical authority for regulated medical supply chain operations. It leads troubleshooting, root-cause analysis, equipment and process performance improvement, validation and change control, and preventive and predictive maintenance planning. It also coordinates technical escalations and business-continuity planning and provides leadership across equipment design, commissioning, qualification, lifecycle support, engineering standards, and team development. The role reinforces safety, cybersecurity, quality, and regulatory compliance and may require up to 15% domestic and international travel.

Requirements

  • Bachelor’s degree in mechanical, industrial, or electrical engineering, or an equivalent field.
  • At least 4 years of relevant experience supporting a warehousing or manufacturing environment.
  • At least 1 year of experience with the MAXIMO application, including configuration and administration.
  • Lean Six Sigma Green Belt certification.
  • At least 3 years managing Lean/Six Sigma projects with demonstrated business impact.
  • Project management experience, including control of information flows, budget management/control, and follow-up planning.
  • Use of Good Manufacturing/Distribution principles (GMP) is required.
  • Ability to lead and motivate people and coach them to develop and grow.
  • Presentation and well-developed communication skills.

Nice To Haves

  • Lean Six Sigma Black Belt.
  • Knowledge of FPX methodology.
  • Experience in healthcare, medical device, pharmaceutical, or other regulated environments.
  • FPX, Six Sigma, or Lean training.

Responsibilities

  • Serve as the process engineering technical authority, delivering scalable and compliant solutions for regulated medical supply chain operations.
  • Lead troubleshooting and root-cause analysis for sortation, conveyance, PLC, HMI, drives, sensors, safety systems, and controls networks to restore uptime and prevent recurrence.
  • Manage equipment and process KPIs, including availability, throughput, cycle time, MTBF, MTTR, quality, and cost, to improve reliability and service performance.
  • Develop validation and change-control strategies for equipment, controls, software, and process modifications, including risk assessment, testing, approval, training, and regulatory compliance.
  • Drive Lean Six Sigma, statistical, and failure-mode analyses to improve capacity, product flow, labor utilization, and operational resilience.
  • Define preventive and predictive maintenance strategies, critical spares, obsolescence plans, maintenance windows, and recovery procedures for business-critical assets.
  • Lead technical escalations and business-continuity planning by coordinating internal teams and vendors through containment, recovery, root-cause confirmation, and closure.
  • Provide technical leadership across equipment design, commissioning, qualification, lifecycle support, engineering standards, and team development while reinforcing safety, cybersecurity, quality, and compliance.
  • Lead and motivate people and coach them to develop and grow.
  • Travel up to 15% domestically and internationally as required.
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